Participants must, in the opinion of the investigator, be capable of complying with the protocol
The subject is capable of understanding and complying with the protocol and has signed the informed consent document
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
The subject is capable of understanding and complying with the protocol and has signed the informed consent document
The subject is capable of understanding and complying with the protocol and has signed the informed consent document
The subject is capable of understanding and complying with protocol requirements.
The subject is capable of understanding and complying with the protocol and has signed the informed consent document
Participants must in the opinion of the investigator be capable of complying with this protocol
The participant is capable of understanding and complying with the protocol and has signed the informed consent document
In the opinion of the Investigator, the patient is capable of understanding and complying with the protocol and has signed the informed consent document.
Capable of understanding and complying with protocol requirements.
Participants must, in the opinion of the Investigator, be capable of complying with the requirements of this protocol including self-administration of study treatment
Capable of understanding and complying with the protocol requirements and has signed the informed consent document.
The participant is capable of understanding and complying with the protocol and has signed the informed consent document
Must be willing and capable of understanding and cooperating with the requirements of the study.
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Capable of understanding and complying with the protocol and has signed the informed consent document
The patient is capable of understanding and complying with the protocol and has signed the informed consent document. A signed informed consent form must be obtained before any study-specific procedures are performed.
mCRPC EXPANSION COHORT: Patient must be capable of understanding and complying with protocol requirements and is willing to give informed consent
Subject is capable of understanding the informed consent process
Capable of understanding and complying with the protocol requirements and has signed the informed consent document
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Capable of understanding the informed consent and complying with the protocol and signed the informed consent document prior to any study-specific screening procedures or evaluations being performed
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Capable of understanding and complying with the protocol requirements and has signed the informed consent document
Participant must be capable of understanding and complying with the protocol and willing to sign a written informed consent document
Patient must be capable of understanding and complying with protocol requirements and is willing to give informed consent
Capable of understanding and complying with the protocol requirements and has signed the informed consent document
Capable of understanding and complying with the protocol requirements and has signed the informed consent document
The subject is capable of understanding and complying with parameters as outlined in the protocol
Patient must be capable of understanding and complying with protocol requirements and is willing to give informed consent
The participant is capable of understanding and complying with the protocol requirements and has signed the informed consent document
The subject is capable of understanding and complying with parameters as outlined in the protocol
In the opinion of the investigator, the participant or legal guardian is capable of understanding and complying with protocol requirements for the duration of the study.
Participants must, in the opinion of the investigator, be capable of complying with the protocol
Must in the opinion of the investigator be capable of complying with this protocol
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Participants must, in the opinion of the investigator, be capable of complying with the protocol
Written voluntary informed consent: the patient is capable of complying with the requirements of the written Informed Consent Form and complying with protocol requirements
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Subjects must in the opinion of the Investigator be capable of complying with this protocol
Participants must be capable of understanding and complying with the protocol requirements and signing informed consent
Participants must, in the opinion of the investigator, be capable of complying with the requirements of this protocol
Capable of complying with study procedures and communicating with study personnel
Patient is capable of complying with study procedures
Patient is capable of complying with study procedures
Patient is capable of complying with study procedures
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
Patient is capable of complying with study procedures
Capable of understanding and complying with protocol requirements.
The patient is capable of understanding and complying with the protocol and has signed the informed consent document.
Ability to provide informed consent and adhere to the required follow-up
Ability to provide informed consent
Ability to provide informed consent
Ability to provide informed consent.
Ability to provide informed consent for participation
Ability to provide informed consent
Ability of patient to provide informed consent
Ability to provide informed consent.
Ability to provide informed consent
Ability to provide informed consent
Ability to provide informed consent
Ability and willingness to provide informed consent to participate in this study
Ability to provide informed consent
Ability to provide informed consent
Ability to provide informed consent
Ability to provide informed consent
Ability to provide informed consent
Ability to provide informed consent
Ability and willingness to provide informed consent
Ability to provide informed consent
Patient has the ability and willingness to provide informed consent and has signed the informed consent document
Ability to provide informed consent
Ability to provide informed consent
Ability to provide informed consent.
Ability to provide informed consent
Ability to provide informed consent
Ability to provide informed consent
Ability to provide informed consent
The ability to provide informed consent
Ability to provide informed consent
Ability to provide informed consent
Ability and Willingness to provide informed consent
Ability to provide informed consent
Have the ability to provide informed consent in English
FOLLOW UP ASSESSMENTS: Have the ability to provide informed consent in English
the ability to comply with the study protocol and provide informed consent
Ability to provide informed consent
Ability to provide informed consent
Ability to provide informed consent
Ability to provide informed consent
Ability to provide consent
PATIENTS: The ability to provide informed consent
Ability to comply with the study protocol, in the investigator's judgment
Ability and willingness to comply with the study protocol for the duration of the study and with follow-up procedures.
Ability and willingness to comply with the requirements of the study protocol
Patient must have the ability to comply with all study requirements
Ability to comply with study procedures in the Investigator's opinion
Ability to comply with the study protocol, in the investigator's judgment
Willingness and ability to comply with study and follow-up procedures.
Willingness and ability to comply with study and follow-up procedures
Ability to comply with the study protocol, in the investigator's judgment
Limitation of the patient's ability to comply with the treatment or follow-up protocol.
Ability to comply with the protocol
Willingness and ability to comply with protocol-specified Pneumocystis jirovecii pneumonia (PJP) prophylaxis
Willingness and ability to understand the nature of this study and to comply with the study and follow-up procedures.
Willingness and capability to comply with the requirements of the study.
Ability and willingness to comply with the requirements of the study protocol
Willingness and ability to comply with study procedures and follow-up examination
Willingness and ability of the subject to comply with study activities.
Ability to comply with treatment, PK and test schedules
STUDY ENTRY: Ability and willingness to comply with the requirements of the study protocol.
Ability to comply with the study protocol, in the investigator's judgment
Willingness and ability to comply with the trial and follow-up procedures.
Ability to comply with all study procedures and willingness to remain supine for 120 minutes during imaging
Ability to comply with the protocol
Stated willingness to comply with study procedures and duration.
Ability to comply with the protocol
Ability and willingness to comply with the requirements of the study protocol
Ability and willingness to comply with the requirements of the study protocol
Ability to comply with the protocol
Stated willingness to comply with all study procedures and be available for the duration of the trial
Ability to comply with protocol requirements.
Ability to comply with the protocol.
Ability and willingness to comply with the requirements of the study protocol
Willingness and ability of subject to comply to study requirements
Ability and willingness to comply with the requirements of the study protocol
Ability and willingness to comply with the requirements of the study protocol
Ability to give informed consent and comply with the protocol
Patients must sign informed consent form (ICF) and show ability and willingness to comply with the requirements of the study protocol
Willingness and ability to comply with all study procedures and able to take oral medications
Willingness and ability to comply with study procedures and follow-up examinations
Ability to comply with the protocol
In the investigator’s opinion, the patient has the ability to communicate satisfactorily with the investigator, to participate fully in the study, and comply with all its requirements
Ability to comply with requirements of the protocol, as assessed by the investigator by the patient signing the consent form
Ability to swallow study drugs and to comply with study requirements throughout the study
Willingness to comply with study guidelines
Ability to comply with the protocol procedures (including geographic accessibility)
Have the ability to understand and comply with the requirements and follow-up time points of the study
Willingness and ability to comply with study and follow-up procedures
Willingness and ability to comply with study and follow-up procedures.
Ability and willingness to comply with the requirements of the study protocol.
Ability to give informed consent and comply with the protocol
Ability and willingness to comply with the requirements of the study protocol
Have the willingness and ability to understand the nature of this study and to comply with the study and follow-up procedures.
State willingness to comply with all study procedures and be available for the duration of the trial
Ability and willingness to comply with the requirements of the study protocol
Ability to give written informed consent and willingness to comply with the requirements of the protocol
Ability and willingness to comply with all study requirements
Limitation of the patient's ability to comply with the treatment or to follow-up the protocol.
Have the willingness and ability to comply with scheduled visit and study procedures.
Ability to comply with the study protocol, in the investigator’s judgment
Limitation of the patient's ability to comply with the treatment or follow-up requirements.
Ability and willingness to provide written informed consent, and to comply with the requirements of the protocol
Ability to comply with endometrial biopsies every 3 months
Ability to comply with study procedures
Ability and willingness to comply with the requirements of the study protocol
Ability and willingness to comply with the requirements of the study protocol
Willingness and ability to comply with study and follow-up procedures.
Ability and willingness to comply with the requirements of the study protocol
Ability to give written informed consent and willingness to comply with the requirements of the protocol
Ability to give written informed consent and willingness to comply with the requirements of the protocol
Ability to comply with study procedures, in the Investigator's opinion
Ability and willingness to comply with the requirements of the study protocol
Stated willingness of patient to comply with study procedures and reporting requirements.
Ability to comply with endometrial biopsies every 3 months
Ability and willingness to comply with the requirements of the study protocol
Ability to swallow study drugs and to comply with study requirements throughout the study.
Willingness and ability to comply with study and followup procedures.
Willingness and ability to comply with study and follow-up procedures
Ability to comply with an oral drug regimen
Any condition that would interfere with the ability to give informed consent or comply with the study protocol
Ability and willingness to comply with the requirements of the study protocol
Ability and willingness to comply with study visits, treatment, testing, and to comply with the protocol, in the investigator's judgment
Willingness and ability to provide written informed consent and to comply with the protocol requirements
Ability to comply with the protocol
Willingness and ability to comply with all study procedures
Written informed consent (and assent when applicable) obtained from subject and ability for subject to comply with the requirements of the study, including the ability to read and speak English.
Any condition that, in the opinion of the enrolling investigator, would interfere with the subject’s ability to comply with the study requirements
Ability to understand and comply with the requirements of this study
Ability to understand and comply with study guidelines
Willingness to comply with study guidelines
Willingness to comply with all study interventions and follow-up procedures including the ability to apply the study drug to the breast
Ability to comprehend and comply with the requirements of the Study
Willingness to comply with all study interventions and follow-up procedures including the ability to swallow the study drug
Willingness to comply with study guidelines
Has any condition that interferes with the ability of the subject to understand or comply with the requirements of the study.
Willingness to comply with the study protocol
Ability to provide signed informed consent and willingness to comply with protocol requirements
Ability and willingness to comply with the study procedures
Willingness to comply with the requirements of the study
Limitation of the patient's ability to comply with the treatment or follow-up protocol.
Willingness and ability to comply with the trial and follow-up procedures.
Willingness and ability to comply with study procedures
As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures for the entire length of the study
COHORT 1: As determined by the enrolling physician or protocol designee, ability of the patient to understand and comply with study procedures for the entire length of the study
COHORT 2: As determined by the enrolling physician or protocol designee, ability of the patient to understand and comply with study procedures for the entire length of the study
As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures for the entire length of the study
As determined by the enrolling physician or protocol designee, ability of the patient to understand and comply with study procedures for the entire length of the study
As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures for the entire length of the study.
As determined by the enrolling physician or protocol designee, willingness and ability of the subject to understand and comply with study procedures
As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures for the entire length of the study
As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures for the entire length of the study.
As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures for the entire length of the study
CELL PROCUREMENT: As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures
LYMPHODEPLETION: As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures
iC9-CAR19 CELL INFUSION: As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures
Able to understand and comply with protocol requirements for the entire length of the study
As determined by the enrolling physician or protocol designee, ability of the patient to understand and comply with study procedures for the entire length of the study
Ability to understand and comply with study procedures for the entire length of the study as determined by the site investigator or protocol designee
As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures for the entire length of the study.
As determined by the enrolling physician or protocol designee, the subject should be able to understand and comply with study procedures for the entire length of the study
As determined by the enrolling physician or protocol designee, ability of the patient to understand and comply with study procedures for the entire length of the study
As determined by the enrolling physician or protocol designee, ability of the patient to understand and comply with study procedures for the entire length of the study
As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures for the entire length of the study
Ability to understand study procedures and to comply with them for the entire length of the study
Be able to understand study procedures and comply with them for the entire length of the study period
Ability to understand and comply with study procedures for the entire length of the study
Ability to comply with study procedures for the entire length of the study
Ability to understand study procedures and to comply with them for the entire length of the study
As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures for the entire length of the study
Must be able to understand and comply with study procedures for the entire length of the study
Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception for the subject; as determined by the enrolling physician or protocol designee, ability of the patient to understand and comply with study procedures for the entire length of the study
As determined by the enrolling physician or protocol designee, ability of the patient to understand and comply with study procedures for the entire length of the study
Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study.
Have mental deficits and/or psychiatric history that may compromise the ability to give written informed consent or to comply with the study protocol.
Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study
Mental incompetence or criminal incarceration
Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study
Have mental deficits and/or psychiatric history that may compromise the ability to give written informed consent or to comply with the study protocol.
Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study.
Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study
Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study
Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study
Mental impairment that may compromise compliance with the requirements of the study.
Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study.
Any condition that may compromise the ability to give written informed consent or to comply with the study protocol.
Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study.
Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study
Voluntary written informed consent
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol
Voluntary signed informed consent (IC)
Voluntary written informed consent and HIPAA authorization and agree to comply with all protocol-specified procedures and follow-up evaluations
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol
Voluntary written informed consent
Written and voluntary informed consent.
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol
Voluntary written consent prior to the performance of any research related procedures
Voluntary written consent
Voluntary written consent prior to the performance of any research related procedures
Voluntary written consent prior to the performance of any research related procedures
Voluntary written consent (and assent if donor < 18 years of age) prior to the performance of any research related procedure
Voluntary written consent
Inability to give voluntary informed consent
Voluntary written informed consent
Voluntary written consent before any research related procedures or therapy
Voluntary written consent
Gives voluntary informed consent
Written and voluntary informed consent
Written voluntary informed consent
Written voluntary informed consent
Written voluntary informed consent
Written voluntary informed consent
Voluntary written informed consent and HIPAA authorization and agree to comply with all protocol-specified procedures and follow-up evaluations
Voluntary written consent prior to the performance of any research related procedures
Voluntary written consent
Voluntary written consent
Voluntary written consent (adult or parental/guardian)
Voluntary written consent prior to the performance of any research related procedures
DONORS: Voluntary written consent prior to the performance of any research related procedure
Voluntary written consent
DONOR: Voluntary written consent
DONOR: Voluntary written consent
DONOR: Voluntary written consent
Voluntary written informed consent
Voluntary written consent
Voluntary written consent
Ability to give voluntary informed consent and to comply with treatment and required tests
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol.
Voluntary written informed consent of the patient (both to participate in the study and to provide biopsy samples) obtained before any study-specific procedure.
Written, voluntary informed consent.
Able to sign voluntary written informed consent
Voluntary written consent
Voluntary written consent
Gives voluntary informed consent
Voluntary written consent
Voluntary written consent
DONOR: Voluntary written consent
Voluntary consent form
Voluntary written consent
DONOR: Voluntary written consent
Voluntary written consent
DONOR: Voluntary written consent
Written and voluntary informed consent
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol
Voluntary written informed consent
Written, voluntary informed consent
Voluntary written consent
Able and willing to give voluntary, written and signed, informed consent
Voluntary, written informed consent.
Voluntary written informed consent
DONOR: Voluntary written consent
Voluntary written consent
Voluntary signed, written IRB-approved informed consent.
Voluntary written consent must be given before performance of any study-related procedure
Voluntary written informed consent
Voluntary written consent must be given before performance of any study-related procedure
Voluntary written consent
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol.
Voluntary agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol
Voluntary, signed informed consent
Are able to provide voluntary, written consent
Voluntary written consent
Voluntary written consent
Voluntary written consent
Voluntary written consent prior to the performance of any research related procedures
Able to give voluntary written informed consent